Patent Application
20190135887
The present invention concerns metabolically stable and non-immunogen spexin analogs that are completely soluble at physiological pH, and their use for the prevention or the treatment of diseases mediated by the galanin receptor 2 (GALR2).
The galanin receptor 2 (GALR2), belonging to G-protein coupled receptors (GPCRs) responsible for transducing a signal within a cell, was isolated from rat hypothalamus extract (Howard et al., FEBS Letts., 405: 285-290, 1997; Smith et al., J. Biol. Chem. 272: 24612-24616, 1997; Wang et al., Mol. Pharmacol., 52: 337-343, 1997) [1-3]. This receptor couples to Gl/Go, Gq/G11 or G12 G-protein types, which means that this subtype of galanin receptors can mediate stimulatory as well as inhibitory effects. The distribution of GALR2 is widespread within the CNS but different from that of GALR1. The dorsal root ganglia (DRG) expresses the highest level of GALR2 in the rat (O'Donnell et al., J. Comp. Neurol., 409: 469-481, 1999; Waters et Kraus, Neurosci., 95: 265-271, 2000) [4, 5], while low levels of GALR2 mRNA were detected in the rat locus coeruleus (LC) and in the dorsal raphe nucleus (DRN) region (O'Donnell et al., J. Comp. Neurol., 409: 469-481, 1999) [4]. The mouse GALR2 has been reported in the mouse brain but not in the DRN (Hawes et al., J. Comp. Neurol., 479: 410-423, 2004) [6]. Although GALR2 is known to display a function particularly in anxiety, depression, appetite regulation and pain modulation the further determination of its functions would benefit from a stable and selective agonist that acts only at GALR2.
Neuropeptide Q, alias Spexin, is a hormone recently discovered by Mirabeau et al. (Genome Res., 17: 320-327, 2007) [7]. The authors developed a Hidden Markov Model (HMM) based on algorithm searches that integrates several peptide hormone sequence features to identify novel peptide hormone. The predicted mature spexin peptide sequence of 14 amino acids flanked by dibasic cleavage sites is evolutionarily conserved across vertebrate species. Spexin expression in brain regions and peripheral tissues of various mammals suggests multiple physiological functions for spexin. Recently spexin was implicated in regulation of feeding behaviors and related metabolic processes (Walewski et al., Obesity 22:1643-1652, 2014) [11]. In addition, spexin is likely involved in reproduction, cardiovascular/renal function, and nociception (Liu et al., Mol. Cell Endocrinol., 374(1-2): 65-72, 2013; Toll et al., Faseb J., 26:947-954, 2012) [12, 13]. However the precise roles of spexin in these processes were not well understood due a lack of information on the spexin receptor.
More recently it has been found that spexin is an endogenous ligand that acts at GALR2 and GALR3 but not at GALR1 (Kim et al., Endocrinol., 155: 1864-1873, 2014) [8]. Based upon the GALR2/spexin interaction, it has been proposed to develop screening assays for agents modulating the activity of the GALR2 and diagnostic assays, as well as kits for performing the same (International Application WO 2012/042455) [9].
Considering the interaction between Spexin and galanin receptors, development of more stable and subtype-selective GALR2 agonists would lead to marked progress in treatment of galanin receptors-related diseases or disorders, in particular of GALR2-related diseases or GALR2-related disorders. Therefore it has been developed spexin-based human GALR2 specific agonists with increased stability in serum and anxiolytic effect in mice (Reyes-Alcaraz et al., Scientific Reports, 6: 21453, DOI: 10.1038/srep21453, Feb. 24, 2016) [10].
The present invention relates to novel metabolically stable fluoropeptides derived from the Neuropeptide Q, alias Spexin. Such spexin analogs are non-immunogen, completely hydrosoluble at physiological pH and have a better affinity toward GALR2 than the endogenous Neuropeptide Q they derived from. There is a therapeutic interest of using said metabolically stable analogs as therapeutic agents useful for the treatment of GALR2-related diseases or GALR2-disorders, for example central nervous System (CNS) disorders or cardiovascular disorders.
In one aspect, the present invention relates to a spexin analog having the following peptide of formula (I):
Xaa1-Trp-Xaa2-Xaa3-Gln-Ala-Xaa4-Xaa5-Tyr-Leu-Lys-Gly-Xaa6-Xaa7 (I)
wherein said peptide of formula (I) (SEQ ID NO: 1) is covalently linked to a fluorocarbon group, directly or through a linker selected from the group consisting of a PEG or a peptide having from 1 to 6 amino acids, either on the alpha-amino or the epsilon-amino group of at least one lysine of the peptide formula (I), and when the spacer is a lysine, the fluorocarbon group is directly linked to the epsilon-amino group of said spacer, and wherein:
Said spexin analog is advantageously metabolically stable, non-immunogen analog, and completely hydrosoluble at physiological pH.
As used herein, the expression “completely hydrosoluble at physiological pH” means that the fluoropeptides of the present invention as above described have at least 50% hydrophobic amino acid residues and have an overall positive net charges and a final solubility in aqueous mixture above 100 μM by visual inspection of the cloudiness of the resulting dispersion and/or solubility measurements by classical physicochemical methods.
As used herein, the expression “non-immunogen” means that the fluoropeptides of the present invention as above described are not derived from any antigens capable of inducing immune response in an animal, including humans. Antigens may be derived from a virus, bacterium or mycobacterium, parasite, fungus, or any infectious agent or an autologous antigen or allergen. The fluoropeptides described in the invention are not included in any vaccine.
As used herein, the expression “metabolically stable” means that the fluoropeptides of the present invention as described above, have at least the half-life of the native peptide, and in particular when linked to a charged linker, have a half-life at least twice longer than native peptide, of at least 20 min or more than one hour, as measured in the stability assay performed in human plasma.
As used herein, the term “fluorocarbon” includes either, perfluorocarbon (where all hydrogen are replaced by fluor) or, hydrofluorocarbon (which contains both C—H and C—F bonds).
The fluorocarbon group may comprise one or more chains derived from perfluorocarbon or mixed fluorocarbon/hydrocarbon radicals, and may be saturated or unsaturated, each chain having from 3 to 30 carbon atoms. The fluorocarbon group is linked to the peptide through a covalent linkage, for example via NH2-group of a lysine of the peptide of formula (I). The coupling to the peptide may be achieved through a functional group for linkage to —NH2, being naturally present on the lysine of the peptide of formula I, or onto a linker. Modify the nature of the linkage between the fluorocarbon chain and the peptide allows modulating the stability and/or solubility of the peptide. Examples of such linkages between the fluorocarbon chain and the peptide of formula I include amide, hydrazine, disulphide, thioether, ester and oxime bonds.
Optionally, a cleavable linker element (peptide or non-peptidic) may be incorporated to permit cleavage of the peptide of formula I from the fluorocarbon group. The linker may also be incorporated to assist in the synthesis of the fluoropeptide and to improve its stability and/or solubility, for example by including additional charges. So charged linker may be particularly useful especially if the peptide to which it is linked has no cationic aminoacids (i.e. lysine, histidine, arginine) at its N-terminal end. Examples of linkers include polyethylene glycol (PEG), or a peptide having about 1 to 6 amino acids, natural on non-natural ones, that may be cleaved by proteolytic enzymes or not. Preferably said amino acids are chosen from the group consisting of basic or aliphatic amino acids, more preferably from histidine, lysine, arginine and glycine. For example, the linker may be Arg-Gly-Arg.
Thus, the fluorocarbon group of the spexin analog of the present invention has chemical formula (II) CmFn—CyHx(L) wherein m=3 to 30, n≤2m+1, y=0 to 2, x≤2y, (m+y)=3 to 30, and L, which is optional, is a functional group leading to covalent attachment to the peptide. For example said functional group is a carbonyle —C(O)— that forms an amide bond with the —NH2 of a lysine.
According to a particular embodiment of the above formula II of the fluorocarbon, m=5 to 15, preferably m=5 to 15 and y=1 to 4. According to another particular embodiment, the formula of the fluorocarbon group is perfluoroundecanoic acid of formula (A)
or alternatively is 2H,2H,2H,3H,3H-perfluoroundecanoic acid of formula (B)
or alternatively is heptadecafluoro-pentadecanoic acid of formula (C)
In these cases it is to be noted that reducing the length of the fluorocarbon group of formula (II), for example by deleting at least two CF2 groups, preferably at least four CF2 groups, can increase the solubility and/or plasmatic stability of the peptide of formula (I) to which it is linked.
According to a particular embodiment, the spexin analog of formula (I) as above defined is further covalently linked to an acetyl group and/or an acyl group —C(O)R where R is a C7-30 alkyl. For example it has the following formula (III) CH3—CyHx-C(O)— wherein y=7 to 30, preferably y=10 to 20, more preferably y=14, and x=2y.
Said fluorocarbon group or further acetyl and:or acyl group can be linked at the N-terminal part of the peptide directly through a lysine, either on the alpha-amino or the epsilon-amino groups.
According to a particular embodiment of a fluoropeptide of formula (I), the present invention relates to a spexin analog selected from the group consisting of:
v) a spexin analog with an amino acid sequence having at least 80% identity with the sequence of (i), (ii), (ii) or (iv).
In another aspect, the present invention also relates to a pharmaceutical composition comprising a spexin analog of formula (I) as above described, and one or more pharmaceutically acceptable excipient.
Such pharmaceutical composition is prepared for administration to a subject in need thereof and which include therapeutically effective amount of one or more of the metabolically stable spexin analog(s) of the present invention. The therapeutically effective amount of a metabolically stable spexin analog will depend on the route of administration, the type of mammal that is the subject and the physical characteristics of the subject being treated. Specific factors that can be taken into account include disease severity and stage, weight, diet and concurrent medication. The relationship of these factors to determining a therapeutically effective amount of the disclosed compounds is well known and understood by those of ordinary skill in the art. Pharmaceutically acceptable excipients or vehicles are also well known to those of ordinary skill in the art. Standard excipients include solutions such as sterile water, saline, and buffered solutions at physiological pH. For example, pharmaceutical excipients include thickeners, diluents, buffers, preservatives, surface active agents and the like in addition to the spexin analog of choice. The pharmaceutically composition can be prepared in the form of aqueous solutions, lyophilized or other dried formulations (powder, granules, lozenges, etc . . . ). In general the nature of the excipient or vehicle will depend on the particular mode of administration being employed. The pharmaceutically composition can be administered intravenously, intramuscularly, subcutaneously, intracerebroventricularly, orally, intraperitoneally, etc . . . or in an aerosol form.
The dosing is selected by those of ordinary skill in the art so that a therapeutically effect is achieved, and depends on the route of administration and the dosage form that is used. Total daily dose of a peptide administered to a subject in single or divided doses may be in amounts, for example, of from about 0.001 to about 100 mg/kg body weight daily, preferably 0.01 to 10 mg/kg/day. Dosage unit compositions may contain such amounts of such submultiples thereof as may be used to make up the daily dose. It will be understood, however, that the specific dose level for any particular patient will depend upon a variety of factors including the body weight, general health, sex, diet, time and route of administration, rates of absorption and excretion, combination with other drugs and the severity of the particular disease being treated.
In another aspect, the present invention also relates to a spexin analog of the present invention, for use as a drug.
In another aspect, the present invention also relates to a spexin analog of the present invention, for use in the prevention or treatment of a GALR2-related disease or GALR2-related disorder, preferably selected from central nervous system (CNS) disorders, cardiovascular disorders, nociception, renal disorders, neuroinflammation, etc . . . . For example said diseases or disorders include, but are not limited to:
The present invention will be further illustrated by the following figures and examples. However these examples and figures should not be interpreted in any way as limiting the scope of the present invention.
Reagents were obtained from commercial source and used without any further purification. Fmoc-L-amino acids were purchased from Novabiochem, Polypeptides and Iris Biotech. Fmoc-protected Rink Amide NovaGel® resin was purchased from Novabiochem and the overall yields for the solid-phase syntheses were calculated based on the initial loadings provided by the supplier (0.7 mmol/g). Fmoc-protected Wang NovaGel® resin was purchased from Novabiochem and the overall yields for the solid-phase syntheses were calculated based on the initial loadings provided by the supplier (0.1 mmol/g).
Analysis were performed either on a C18 Sunfire column (5 μm, 4.6 mm×150 mm) using a linear gradient (5% to 95% in 20 min, flow rate of 1 mL.min−1) of solvent B (0.1% TFA in CH3CN, v/v) in solvent A (0.1% TFA in H2O, v/v). Detection was set AT 220 nm and 254 nM.
Purifications were performed on Sunfire C18 column (5 μm, 19×150 mm) on Gilson PLC2020 with absorption detection. The separation was achieved using successive isocratic and linear gradients (5min at 5%; 5% to 60% in 30 min; 60% to 100% in 10 min; flow rate of 20 mL.min−1) of solvent B (0.1% TFA in CH3CN, v/v) in solvent A (0.1% TFA in H2O, v/v).
Analysis were obtained on a ZQ (Z quadripole) Waters/Micromass spectrometer equipped with an X-Terra C18 column (0.5 μm, 4.6 mm×50 mm) using electrospray ionization mode (ESI).
Analysis were acquired on a Bruker MicroTof mass spectrometer, using electrospray ionization (ESI) and a time-of-flight analyzer (TOF) or on an Autoflex II TOF/TOF Bruker mass spectrometer using matrix-assisted laser desorption/ionization technique (MALDI) and a time-of-flight analyzer (TOF).
Standard automated solid-phase peptide synthesis (SPPS) were performed on an Applied Biosystem ABI 433A synthesizer (Appelar, France). The elongation was carried out by coupling a 10-fold excess of Fmoc-L-amino acid derivatives, using 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (HBTU), 1-hydroxybenzotriazole (HOBt), and diisopropylethylamine (Hünig's base) (DIPEA) as coupling reagents in N,N-dimethylformamide (DMF) as solvent. At the end of the peptide sequence synthesis, the resin was washed with CH2Cl2 and MeOH and then dried in vacuo. After each coupling step, Fmoc deprotection was performed by treatment with piperidine monitored by UV at 301 nm.
Peptide elongation was performed starting from fried resin previously synthetized by standard automated SPPS. Non-automated SPPS were performed in polypropylene tubes equipped with polyethylene frits and polypropylene caps using an orbital agitator shaking device.
The Fmoc-protected resin (1 equiv) was swollen 1 h in DMF and the excess solvent was removed by filtration. Cleavage of the Fmoc protecting group was performed in a solution of 20% (v/v) piperidine in DMF (2 times for 15 min). The piperidine solution was drained off and the resin was washed with successively DMF, CH2Cl2 and MeOH (3×0.5 mL).
All Fmoc-protected amino acids (4 equiv) were coupled in N,N-dimethylformamide (DMF) for 45 min using HBTU (3.8 equiv) and HOBt (4 equiv) with N,N-diisopropylethylamine (DIEA) (12 equiv) as activating agents. The excess solvent was removed by filtration and the resin was washed with successively DMF, CH2Cl2 and MeOH (3×0.5 mL).
The cycle of coupling, washing and deprotection were repeated until the targeted peptides were obtained. The completion of couplings and Fmoc deprotections were monitored with ninhydrin test and TNBS test:
The resin containing the peptide sequence of interest (1 equiv) was swollen in DMF, and the excess solvent was removed by filtration. A solution of piperidine in DMF (20% v/v-0.5 mL) was added, and the mixture was shaken at room temperature for 15 min. The solution was drained, and the operation was repeated for 15 min. The solution was drained, and the resin was washed with DMF and CH2Cl2. In a separate vial, DIEA (8 equiv) was added to a solution of 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-heptadecafluoroundecanoic acid (2 equiv), HBTU (2 equiv), and HOBt (1.9 equiv) in DMF (0.5 mL). The mixture was stirred at room temperature for 1 min and was added to the resin. The mixture was shaken at room temperature for 2 h. The solution was drained and the resin was washed with DMF, CH2Cl2, and MeOH the dried in vacuo.
The dried resin was treated with TFA/Phenol/Thioanisole/1,2-Ethanedithiol/water (10 mL/0.75 g/0.5 mL/0.25 mL/0.5 mL) and the mixture was shaken at room temperature for 3h. The filtrate was collected in a cold diethyl ether solution and the beads washed with TFA. The solution was centrifuged at 3000 rpm for 2 min. The precipitate was washed in a cold diethyl ether solution and centrifuged at 3000 rpm for 2 min. The diethyl ether solution was eliminated and the precipitate was dried in vacuo. The crude product was purified by semi-preparative RP-HPLC and lyophilized.
Fmoc-Asn-Trp-Thr-Pro-Gln-Ala-Met-Leu-Tyr-Leu-Lys-Gly-Ala-Gln-Rink resin (23 μmol), 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-heptadecafluoroundecanoic acid (2 equiv), HBTU (2 equiv), HOBt (1.9 equiv) and DIEA (8 equiv) were reacted according the general procedure, affording the title compound (6.9 mg, 14%) as a white solid. tR=13.60 min (>95% purity at 220 nm); HRMS (ESI) calcd for C85H117F17N20O20S: 2092.82023; found: 2092.81872.
Fmoc-Asn-Trp-Thr-Pro-Gln-Ala-Met-Leu-Tyr-Leu-Lys-Gly-Ala-Gln-Rink resin (29 μmol), Fmoc-Arg(Pbf)-OH (4 equiv), HBTU (3.8 equiv), HOBt (4 equiv) and DIEA (12 equiv) were reacted according the general procedure. Fmoc-Gly-OH (4 equiv) and Fmoc-Arg(Pbf)-OH (4 equiv) were then added with the same procedure. Finally, 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-heptadecafluoroundecanoic acid (2 equiv), HBTU (2 equiv), HOBt (1.9 equiv) and DIEA (8 equiv) were reacted according the general procedure, affording the title compound (10.5 mg, 13%) as a white solid. tR=11.02 min (>95% purity at 220.8 nm); HRMS (ESI) calcd for C99H144F17N29O23S: 2462.04391; found: 2462.05017.
Fmoc-Asn-Trp-Thr-Pro-Gln-Ala-Met-Leu-Tyr-Leu-Lys-Gly-Ala-Gln-Lys(ivDde)-Rink resin (22 μmol) was treated in a solution of 20% (v/v) piperidine in DMF (2 times for 15 min). The piperidine solution was drained off and the resin was washed with successively DMF, CH2Cl2 and MeOH (3×0.5 mL). Acetylation of NH2-Asn-Trp-Thr-Pro-Gln-Ala-Met-Leu-Tyr-Leu-Lys-Gly-Ala-Gln-Lys(ivDde)-Rink resin was performed by adding 0.5 mL of a solution of 10% anhydride acetic and 5% DIEA in CH2Cl2 for 10 min. The acetylation solution was drained off and the resin was washed with 0.5 mL of CH2Cl2 for 2 min (3 times). Removal of the ivDde protecting group was performed in a solution of 2% (v/v) hydrazine in DMF (3 times for 3 min). The hydrazine solution was drained off and the resin was washed with successively DMF, CH2Cl2 and MeOH (3×0.5 mL). Finally, 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-heptadecafluoroundecanoic acid (2 equiv), HBTU (2 equiv), HOBt (1.9 equiv) and DIEA (8 equiv) were reacted according the general procedure. Following treatment in acidic conditions and precipitation, the crude mixture was purified by RP-HPLC, concentrated under vacuum and freeze-dried, affording the title compound (4.5 mg, 8.6%) as a white solid. tR=13.11 min (>95% purity at 220 nm); HRMS (ESI) calcd for C93H131F17N22O22S: 2262.92709; found: 2262.92680.
Fmoc protecting group of Fmoc-Asn-Trp-Thr-Pro-Gln-Ala-Met-Leu-Tyr-Leu-Lys-Gly-Ala-Gln-Lys(ivDde)-Rink resin (21 μmol) was performed in a solution of 20% (v/v) piperidine in DMF (2 times for 15 min). The piperidine solution was drained off and the resin was washed with successively DMF, CH2Cl2 and MeOH (3×0.5 mL). Acetylation of NH2-Asn-Trp-Thr-Pro-Gln-Ala-Met-Leu-Tyr-Leu-Lys-Gly-Ala-Gln-Lys(CO(CH2)2C8F17)-Rink resin was performed by adding 0.5 mL of a solution of 10% anhydride acetic and 5% DIEA in CH2Cl2 for 10 min. The acetylation solution was drained off and the resin was washed with 0.5 mL of CH2Cl2 for 2 min (three times). Removal of the ivDde protecting group was performed in a solution of 2% (v/v) hydrazine in DMF (3 times for 3 min). The hydrazine solution was drained off and the resin was washed with successively DMF, CH2Cl2 and MeOH (3×0.5 mL). Fmoc-Arg(Pbf)-OH, Fmoc-Gly-OH and Fmoc-Arg(Pbf)-OH were successively reacted according the general procedure. N-Fmoc removal was followed by the coupling of 4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11-heptadecafluoroundecanoic acid according the general procedure. Following treatment in acidic conditions and precipitation, the crude mixture was purified by RP-HPLC, concentrated under vacuum and freeze-dried affording the title compound (3.1 mg, 5.6%) as a white solid. tR=11.10 min (>95% purity at 220 nm); LCMS calcd for C107H158F17N31O25S: 2632.15; found: 2633.17.
Evaluation of the affinity of compounds for the human galanin GAL2 receptor in transfected CHO cells determined in a radioligand binding assay: Experimental protocol: Cells membrane homogenates (4 μg protein) are incubated for 120 min at 22° C. with 0.05 nM [125I]galanin in the absence or presence of the test compound in a buffer containing 25 mM Tris-HCl (pH 7.4), 10 mM MgCl2 and 0.5% BSA. Nonspecific binding is determined in the presence of 1 μM porcine galanin. Following incubation, the samples are filtered rapidly under vacuum through glass fiber filters (GF/B, Packard) presoaked with 0.3% PEI and rinsed several times with ice-cold 50 mM Tris-HCl using a 96-sample cell harvester (Unifilter, Packard). The filters are dried then counted for radioactivity in a scintillation counter (Topcount, Packard) using a scintillation cocktail (Microscint 0, Packard). The results are expressed as a percent inhibition of the control radioligand specific binding. The standard reference compound is porcine galanin, which is tested in each experiment at several concentrations to obtain a competition curve from which its IC50 is calculated.
Calcium mobilization: CHO cells expressing GalR2 were loaded with 2.5 μM of Fluo-4 AM in the presence of 2.5 mM probenicid. Agonist-evoked increases in intracellular calcium were recorded over time (5 sec intervals over 220 sec) at 37° C. by using a Flexstation III (Molecular Devices, Sunnyvale, Calif., USA). Fluorescence signals were recorded at 520 nm (excitation at 485 nm). Peak amplitudes were normalized to baseline and maximal fluorescence level elicited by 20 μM digitonin, and EC50 were calculated with Graphpad/Prism software.
The solubility of each spexin analogs was evaluated after dissolution in water to reach 100 μM. The resulting solution was vortexed 1 min following by 1 min in bath sonication. Solubility was then assessed by visual observation of the resulting dispersion (Clear/Cloudy and presence of particulates).
This procedure is designed to determine the stability of a test compound in blood or plasma from human or animal species in a 96-well plate format. The test compound is quantified at 5 time points by HPLC-MS/MS analysis. Test concentration: 1 μM with a final DMSO concentration of 0.5%. Experimental protocol: Blood or plasma are pre-warmed at 37° C. water bath for 5 min, followed by addition of the test compound. The incubation is performed in a 37° C. water bath for 2 h. An aliquot of the incubation mixture is transferred to acetonitrile at 0, 0.5, 1, 1.5 and 2 h, respectively. Samples are then mixed and centrifuged. Supernatants are used for HPLC-MS/MS analysis. Reference compounds Propoxycaine and propantheline are tested simultaneously with the test compound in each assay. Analytical methods Samples are analyzed by HPLC-MS/MS using selected reaction monitoring. The HPLC system consists of a binary LC pump with autosampler, a C-18 column, and a gradient. Conditions may be adjusted as necessary. Data analysis Peak areas corresponding to the test compound are recorded. The compound remaining (%) is calculated by comparing the peak area at each time point to time zero. The half-life is calculated from the slope of the initial linear range of the logarithmic curve of compound remaining (%) vs. time, assuming first order kinetics.
The results are presented in table 1 below:
The results show that the spexin analogs tested exhibit a better affinity and efficiency than the native peptide (spexin), and at least the same or better hydrosolubility and/or plasma stability.
The propensity of spexin analogs to bind to Eppendorf protein LoBind tubes was evaluated.
A solution of 10 μM of spexin analogs in solution in HEPES/BSA buffer was added to Eppendorf protein LoBind tubes, stirred for 5 min and vortexed for 2 min. The supernatant was removed from the tube and acetonitrile was added to dissolve the compound adsorbed to the plastic. The amount of peptide recovered was then evaluated by HPLC-MS/MS following the same protocol than above described for plasma stability analysis. The non-specific adsorption of peptides (%) was calculated by comparing the peak area of each compound recovered to that obtained with the same compound in DMSO (prevent the adsorption of the compounds to plastic).
The results are presented in table 2 below:
These results show that the presence of the cationic linker enables to lower the non-specific binding interactions of the fluorospexin to the Eppendorf protein LoBind tubes.
In addition, the RP-HPLC retention time of each compound highlights the importance of the linker to increase the global aqueous solubility of fluorospexin as compared to native spexin.
The effects were examined by using the GloSensor™ cAMP Assay according to manufacturer recommendations (Promega, Madison Wis., USA) with a few modifications. HEK293 cells selected for stable expression of human GALR1 were transfected with pGloSensor™-22F using Lipofectamine 2000 (Thermo Fisher Scientific, Waltham Mass., USA), harvested from culture dish the day following transfection and resuspended (106 cells per mL) in physiological Hepes buffer (10 mM HEPES, 0.4 mM NaH2PO4, 137.5 mM NaCl, 1.25 mM MgCl2, 1.25 mM CaCl2, 6 mM KCl, 5.6 mM glucose and 1 mg/mL bovine serum albumin, pH 7.4) supplemented with 1 mM D-Luciferin (Synchem UG & Co. KG, Felsberg-Altenburg, Germany). Following pre-equilibration for 2 h at 25° C., D-luciferin-loaded cells were distributed (100,000 cells per well) in a white 96-well plate and kinetic recordings of their luminescence level were acquired using a FlexStation II (Molecular Devices, Sunnyvale Calif., USA). Compounds to be tested were injected at various concentrations 10 min before forskolin addition (0.5 μM final concentration) and readings were pursued for 30 min. Experiments were conducted at 25° C. in the presence of 0.1 mM IBMX to prevent the degradation of cAMP by phospodiesterases.
The results are presented in table 3 below:
The results show that, as expected, galanin displayed full agonist activity at GalR1 with an EC50 of 0.8 nM. Spexin and spexin derivatives displayed no agonist activity at GalR1 up to 1 μM.
Tail immersion test: Nociception tests were performed on male, awake C57BL/6N male mice (25-30 g weight; Janvier Labs, France). Animals were housed in groups of five per cage and kept under a 12 h/12 h light/dark cycle at 21±1° C. with ad libitum access to food and water. Experiments were performed during the light-on phase of the cycle. Mice were habituated to the testing room and equipment and handled for 1 week before starting behavioural experiments. The nociceptive thermal threshold of mice was determined using the tail immersion test. Mice were restrained in a grid pocket and their tail was immersed in a thermostated water bath. The latency (in sec) for tail withdrawal from hot water (47±0.5° C.) was taken as a measure of the nociceptive response. In the absence of any nociceptive reaction, a cut-off value of 25 sec was set to avoid tissue damage.
The results are shown in
The results show that intracerebroventricular (icy) injection of 10 nmol of spexin elicited an analgesic effect at 15 and 30 min after injection as revealed by a significant increase in tail immersion withdrawal latencies of the animals compared to baseline threshold (from 10.45±0.53 sec basal threshold to 15.38±0.57 sec at 15 min and 13.06±0.87 sec at 30 min; p<0.01 and p<0.05, respectively).
Icy injection of 1 nmol and 0.1 nmol of LE-144 evoked the same statistically significant analgesia after 15 min and 30 min (1 nmol; baseline: 10.12±0.59 sec, 15 min: 15.58±0.61 sec, 30 min: 13.94±0.75 sec; 0.1 nmol; baseline: 9.99±0.5 sec, 15 min: 14.26±0.93 sec, 30 min: 14.06±0.34 sec).
| Number | Date | Country | Kind |
|---|---|---|---|
| 16305734.2 | Jun 2016 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2017/064803 | 6/16/2017 | WO | 00 |
